156 results on '"Bendahhou, Saïd"'
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2. Proximal Renal Tubular Acidosis in TASK2 K + Channel-Deficient Mice Reveals a Mechanism for Stabilizing Bicarbonate Transport
3. New Structural insights into Kir channel gating from molecular simulations, HDX-MS and functional studies
4. MiRP2 Forms Potassium Channels in Skeletal Muscle with Kv3.4 and Is Associated with Periodic Paralysis
5. Double Trouble Mutations Underlie Mitochondrial Dynamics Disorders in a Severe Form of Charcot-Marie-Tooth Disease
6. Andersen’s syndrome mutants produce a knockdown of inwardly rectifying K+ channel in mouse skeletal muscle in vivo
7. Biological fractionation of lithium isotopes by cellular Na+/H+ exchangers unravels fundamental transport mechanisms
8. Cryo–electron microscopy unveils unique structural features of the human Kir2.1 channel
9. Relationships between Plasma Pyrophosphate, Vascular Calcification and Clinical Severity in Patients Affected by Pseudoxanthoma Elasticum
10. Functional characterization of the inward-rectifier potassium (Kir) channel family in bone cells
11. TWIK1, a unique background channel with variable ion selectivity
12. Bisphosphonates Targeting Ion Channels and Musculoskeletal Effects
13. Task2 Potassium Channels Set Central Respiratory CO₂ and O₂ Sensitivity
14. Integrative Study of the Structural and Dynamical Properties of a KirBac3.1 Mutant: Functional Implication of a Highly Conserved Tryptophan in the Transmembrane Domain
15. Cross Pharmacological, Biochemical and Computational Studies of a Human Kv3.1b Inhibitor from Androctonus australis Venom
16. The inward rectifier potassium channel Kir2.1 is required for osteoblastogenesis
17. A204E mutation in Nav1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs
18. Unexpected Gating Behaviour of an Engineered Potassium Channel Kir
19. Dkk3 is a component of the genetic circuitry regulating aldosterone biosynthesis in the adrenal cortex
20. Keeping hyperactive voltage-gated sodium channels in silent mode
21. Mechanisms underlying a life-threatening skeletal muscle Na+ channel disorder
22. Fate of intracellular retained mutant collagen
23. First Evidence of Kv3.1b Potassium Channel Subtype Expression during Neuronal Serotonergic 1C11 Cell Line Development
24. Sodium Channel Fragments: Contributions to Voltage Sensitivity and Ion Selectivity
25. Corticosteroid-exacerbated symptoms in an Andersenʼs syndrome kindred
26. In vivo and in vitro functional characterization of Andersenʼs syndrome mutations
27. KCNQ1 Gain-of-Function Mutation in Familial Atrial Fibrillation
28. Structural and functional characterization of a human potassium channel, Kir2.1
29. A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation
30. Osteogenic and Chondrogenic Master Genes Expression Is Dependent on the Kir2.1 Potassium Channel Through the Bone Morphogenetic Protein Pathway
31. Enhancement of theShaker B Δ6–46 current by fatty acids depends on the activation of the lipoxygenase metabolic pathway
32. Biophysical Characterization of Two NaV1.4 Mutations Making a Clinical Overlap between the Myotonia-Hyperkalemic and Hypokalemic Periodic Paralysis Clusters of Disorders
33. Substitutions of the S4DIV R2 residue (R1451) in NaV1.4 lead to complex forms of paramyotonia congenita and periodic paralyses
34. Modeling Andersen's Syndrome in Human Induced Pluripotent Stem Cells
35. The K+channel TASK1 modulates β‐adrenergic response in brown adipose tissue through the mineralocorticoid receptor pathway
36. Andersen's syndrome mutants produce a knockdown of inwardly rectifying K channel in mouse skeletal muscle in vivo.
37. Autosomal Recessive Inheritance of Congenital Myasthenic Syndrome is Associated with Skeletal Muscle Sodium Channel Mutations
38. Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis
39. The K+ channel TASK1 modulates β-adrenergic response in brown adipose tissue through the mineralocorticoid receptor pathway.
40. A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation
41. Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation
42. Mechanisms underlying a life-threatening skeletal muscle Na+channel disorder
43. Potassium Channel Silencing by Constitutive Endocytosis and Intracellular Sequestration
44. Task2 potassium channels set central respiratory CO 2 and O 2 sensitivity
45. Invalidation of TASK1 potassium channels disrupts adrenal gland zonation and mineralocorticoid homeostasis
46. Does Sumoylation Control K2P1/TWIK1 Background K+ Channels?
47. Role of hydrophobic residues in the voltage sensors of the voltage-gated sodium channel
48. Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients
49. A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation
50. In vivoandin vitrofunctional characterization of Andersen's syndrome mutations
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